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. 2010 Mar 8;107(12):5658–5663. doi: 10.1073/pnas.0912153107

Fig. 1.

Fig. 1.

Non–Ca2+-conducting Ca2+ channels in larval zebrafish skeletal myotubes. (A) Depolarizing test pulses to potentials unto +70 mV were unable to elicit Ca2+ currents at any potential (n = 14). (B) Robust voltage-dependent α1S gating is indicated by charge movements with a Qmax value of 10.45 ± 0.58 nC/μF and a half-maximal activation of −4.21 ± 1.36 mV (n = 20), assessed by integrating the “ON” component of α1S gating currents (Qon). (C) Depolarization-induced intracellular Ca2+ transients had a (ΔF/F0) max value of 4.44 ± 0.42 with half-maximal activation at −10.39 ± 0.75 mV (n = 17). (D) Also, 10 mM Ba2+ instead of 10 mM Ca2+ as a charge carrier did not awake any current at any potential (n = 6).